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NCT07222397 · ClinicalTrials.gov registry record · NA
2910 nm Erbium-Doped Fluoride Fiber Glass Laser for the Treatment of Advanced Perioral Lines and Wrinkles
A NA study of Lines Skin and Photodamaged Skin, sponsored by FA Corporation.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT07222397 is a NA study of Lines Skin and Photodamaged Skin that is actively recruiting participants, run by FA Corporation. The registered enrollment target is 20 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07222397, a NA study of Lines Skin and Photodamaged Skin, is actively recruiting participants, sponsored by FA Corporation.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective is to assess the efficacy, safety and satisfaction associated with the resurfacing treatment of perioral lines and wrinkles with the 2,910 nm mid-infrared Fiber Laser (UltraClear, Acclaro Medical) using both superficial epidermis ablation capabilities and the deep ablative and coagulative capabilities into the dermis for rejuvenation. Participants will receive up to two treatments spaced 6-8 weeks apart, followed by a 1-month and 3-month follow-up visit during which the device will be evaluated for its effectiveness defined as improvement addressing perioral lines and wrinkles utilizing multiple scales completed by the investigator and blinded Independent Photographic Reviewers (IPRs). Additionally, safety, subjective overall aesthetic improvement and satisfaction will be monitored and tracked.
Conditions Studied
Interventions
- DEVICE Laser Resurfacing
Study Locations (1)
Texas
- Dermatology & Laser Surgery Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2025-03-01 |
| Est. Completion | 2026-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07222397
The ClinicalTrials.gov registry entry for NCT07222397 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is FA Corporation, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Lines Skin appearing as the primary indexed condition, and to 1 intervention - of which Laser Resurfacing is the first listed.
NCT07222397 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT07222397 about?
NCT07222397 is a clinical study titled "2910 nm Erbium-Doped Fluoride Fiber Glass Laser for the Treatment of Advanced Perioral Lines and Wrinkles". The primary objective is to assess the efficacy, safety and satisfaction associated with the resurfacing treatment of perioral lines and wrinkles with the 2,910 nm mid-infrared Fiber Laser (UltraClear, Acclaro Medical) using both superficial epidermis ablation capabilities and the deep ablative and ...
What is the current status of trial NCT07222397?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2025-03-01. Estimated completion is 2026-02.
What conditions does trial NCT07222397 study?
This clinical trial studies the following conditions: Lines Skin, Photodamaged Skin, Rhytids, Wrinkles and Rhytides.
What interventions are being tested in trial NCT07222397?
The interventions under investigation include: Laser Resurfacing (DEVICE).
Who is sponsoring clinical trial NCT07222397?
This trial is sponsored by FA Corporation, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07222397 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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